Phosphorus : an element that could have been called Lucifer / / Mikhail Butusov, Arne Jernelov |
Autore | Butusov Mikhail |
Edizione | [1st ed. 2013.] |
Pubbl/distr/stampa | New York, : Springer, 2013 |
Descrizione fisica | 1 online resource (101 p.) |
Disciplina |
546.712
546.712595 |
Altri autori (Persone) | JernelovArne |
Collana | SpringerBriefs in environmental science |
Soggetto topico |
Phosphorus compounds
Phosphorus |
ISBN | 1-4614-6803-5 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Introduction -- The Role of Phosphorous in the Origin of Life and in Evolution -- Phosphorous in the Organic Life - Cells, Tissues, Organisms -- Phosphorous in Social Life -- Silent Underground Life -- Fertilizers - 100 Years of Supremacy -- Non-Fertilizer Uses of Phosphorous -- Eutrophication -- The Politics of P -- Peak Phosphorous -- Phosphate Recycling or Welcome from Lucifer?. |
Record Nr. | UNINA-9910741193703321 |
Butusov Mikhail
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New York, : Springer, 2013 | ||
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Lo trovi qui: Univ. Federico II | ||
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Phosphorus research bulletin |
Pubbl/distr/stampa | Toyko : , : Japanese Association of Inorganic Phosphorus Chemistry |
Descrizione fisica | 1 online resource |
Soggetto topico |
Phosphorus - Research
Phosphorus compounds - Research Phosphorus Phosphorus compounds |
Soggetto genere / forma | Periodicals. |
ISSN | 1882-2363 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Periodico |
Lingua di pubblicazione | und |
Altri titoli varianti | PRB |
Record Nr. | UNISA-996207882803316 |
Toyko : , : Japanese Association of Inorganic Phosphorus Chemistry | ||
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Lo trovi qui: Univ. di Salerno | ||
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Phosphorus research bulletin |
Pubbl/distr/stampa | Toyko : , : Japanese Association of Inorganic Phosphorus Chemistry |
Descrizione fisica | 1 online resource |
Soggetto topico |
Phosphorus - Research
Phosphorus compounds - Research Phosphorus Phosphorus compounds |
Soggetto genere / forma | Periodicals. |
ISSN | 1882-2363 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Periodico |
Lingua di pubblicazione | und |
Altri titoli varianti | PRB |
Record Nr. | UNINA-9910304534203321 |
Toyko : , : Japanese Association of Inorganic Phosphorus Chemistry | ||
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Lo trovi qui: Univ. Federico II | ||
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Phosphorus(III) ligands in homogeneous catalysis [[electronic resource] ] : design and synthesis / / edited by Paul Kamer & Piet W.N.M. van Leeuwen |
Autore | Kamer Paul |
Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom, : John Wiley & Sons, Ltd., 2012 |
Descrizione fisica | 1 online resource (567 p.) |
Disciplina |
541.2242
546.712595 546/.712595 |
Altri autori (Persone) | LeeuwenP. W. N. M. van (Piet W. N. M.) |
Soggetto topico |
Phosphorus compounds
Ligands Catalysis TECHNOLOGY & ENGINEERING / Material Science |
Soggetto genere / forma | Electronic books. |
ISBN |
1-280-78471-7
9786613695109 1-118-29970-1 1-118-29971-X 1-118-29973-6 |
Classificazione | TEC021000 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Phosphorus( III ) Ligands in Homogeneous Catalysis: Design and Synthesis; Contents; List of Contributors; Preface; 1 Phosphorus Ligand Effects in Homogeneous Catalysis and Rational Catalyst Design; 1.1 Introduction; 1.2 Properties of phosphorus ligands; 1.2.1 Electronic ligand parameters; 1.2.2 Steric ligand parameters; 1.2.3 Bite angle effects; 1.2.4 Molecular electrostatic potential (MESP) approach; 1.3 Asymmetric ligands; 1.4 Rational ligand design in nickel-catalysed hydrocyanation; 1.4.1 Introduction; 1.4.2 Mechanistic insights; 1.4.3 Rational design; 1.5 Conclusions; References
2 Chiral Phosphines and Diphosphines2.1 Introduction; 2.1.1 Early developments; 2.2 Chiral chelating diphosphines with a linking scaffold; 2.2.1 Building chiral backbones from naturally available materials; 2.2.2 Design and synthesis of chiral backbones; 2.2.3 Synthesis from optical resolution of phosphine precursors or intermediates; 2.3 Chiral atropisomeric biaryl diphosphines; 2.3.1 Synthesis of BINAP and its derivatives; 2.3.2 Synthesis of atropisomeric biaryl ligands; 2.3.3 General strategies of synthesizing of atropisomeric biaryl ligands; 2.4 Chiral phosphacyclic diphosphines 2.4.1 Fundamental discovery and syntheses of BPE and DuPhos2.4.2 Design and synthesis of bisphosphetanes; 2.4.3 Design and synthesis of bisphospholanes; 2.4.4 Design and synthesis of bisphospholes; 2.4.5 Design and synthesis of bisphosphinanes; 2.4.6 Design and synthesis of bisphosphepines; 2.4.7 Summary of synthetic strategies of phosphacycles; 2.5 P-stereogenic diphosphine ligands; 2.6 Experimental procedures for the syntheses of selected diphosphine ligands; 2.6.1 Synthesis procedure for DIOP* ligand; 2.6.2 Synthesis procedure of SDP ligands; 2.6.3 Synthesis procedure of (R,R)-BICP 2.6.4 Synthesis procedure of SEGPHOS2.6.5 Synthesis procedure of Ph-BPE; 2.6.6 Synthesis procedure of TangPhos; 2.6.7 Synthesis procedure of Binaphane; 2.7 Concluding remarks; References; 3 Design and Synthesis of Phosphite Ligands for Homogeneous Catalysis; 3.1 Introduction; 3.2 Synthesis of phosphites; 3.2.1 Monophosphites; 3.2.2 Diphosphite ligands; 3.2.3 Triphosphites; 3.3 Highlights of catalytic applications of phosphite ligands; 3.3.1 Hydrogenation reactions; 3.3.2 Functionalization of alkenes: hydroformylation and hydrocyanation 3.3.3 Addition of nucleophiles to carbonyl compounds and derivatives3.3.4 Allylic substitution reactions; 3.3.5 Miscellaneous reactions; 3.4 General synthetic procedures; 3.4.1 Symmetrically substituted phosphites; 3.4.2 Nonsymmetrically substituted phosphites; 3.4.3 Phosphites bearing dioxaphospho-cyclic units; References; 4 Phosphoramidite Ligands; 4.1 Introduction; 4.1.1 History; 4.2 Synthesis of phosphoramidites; 4.3 Reactivity of the phosphoramidites; 4.4 Types of phosphoramidite ligands; 4.4.1 Acyclic monodentate phosphoramidites; 4.4.2 Cyclic monodentate phosphoramidites based on diols 4.4.3 Cyclic phosphoramidites based on amino alcohols |
Record Nr. | UNINA-9910141261103321 |
Kamer Paul
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Chichester, West Sussex, United Kingdom, : John Wiley & Sons, Ltd., 2012 | ||
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Lo trovi qui: Univ. Federico II | ||
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Phosphorus(III) ligands in homogeneous catalysis : design and synthesis / / edited by Paul Kamer & Piet W.N.M. van Leeuwen |
Autore | Kamer Paul |
Edizione | [1st ed.] |
Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom, : John Wiley & Sons, Ltd., 2012 |
Descrizione fisica | 1 online resource (567 p.) |
Disciplina |
541.2242
546.712595 546/.712595 |
Altri autori (Persone) | LeeuwenP. W. N. M. van (Piet W. N. M.) |
Soggetto topico |
Phosphorus compounds
Ligands Catalysis TECHNOLOGY & ENGINEERING / Material Science |
ISBN |
1-280-78471-7
9786613695109 1-118-29970-1 1-118-29971-X 1-118-29973-6 |
Classificazione | TEC021000 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Phosphorus( III ) Ligands in Homogeneous Catalysis: Design and Synthesis; Contents; List of Contributors; Preface; 1 Phosphorus Ligand Effects in Homogeneous Catalysis and Rational Catalyst Design; 1.1 Introduction; 1.2 Properties of phosphorus ligands; 1.2.1 Electronic ligand parameters; 1.2.2 Steric ligand parameters; 1.2.3 Bite angle effects; 1.2.4 Molecular electrostatic potential (MESP) approach; 1.3 Asymmetric ligands; 1.4 Rational ligand design in nickel-catalysed hydrocyanation; 1.4.1 Introduction; 1.4.2 Mechanistic insights; 1.4.3 Rational design; 1.5 Conclusions; References
2 Chiral Phosphines and Diphosphines2.1 Introduction; 2.1.1 Early developments; 2.2 Chiral chelating diphosphines with a linking scaffold; 2.2.1 Building chiral backbones from naturally available materials; 2.2.2 Design and synthesis of chiral backbones; 2.2.3 Synthesis from optical resolution of phosphine precursors or intermediates; 2.3 Chiral atropisomeric biaryl diphosphines; 2.3.1 Synthesis of BINAP and its derivatives; 2.3.2 Synthesis of atropisomeric biaryl ligands; 2.3.3 General strategies of synthesizing of atropisomeric biaryl ligands; 2.4 Chiral phosphacyclic diphosphines 2.4.1 Fundamental discovery and syntheses of BPE and DuPhos2.4.2 Design and synthesis of bisphosphetanes; 2.4.3 Design and synthesis of bisphospholanes; 2.4.4 Design and synthesis of bisphospholes; 2.4.5 Design and synthesis of bisphosphinanes; 2.4.6 Design and synthesis of bisphosphepines; 2.4.7 Summary of synthetic strategies of phosphacycles; 2.5 P-stereogenic diphosphine ligands; 2.6 Experimental procedures for the syntheses of selected diphosphine ligands; 2.6.1 Synthesis procedure for DIOP* ligand; 2.6.2 Synthesis procedure of SDP ligands; 2.6.3 Synthesis procedure of (R,R)-BICP 2.6.4 Synthesis procedure of SEGPHOS2.6.5 Synthesis procedure of Ph-BPE; 2.6.6 Synthesis procedure of TangPhos; 2.6.7 Synthesis procedure of Binaphane; 2.7 Concluding remarks; References; 3 Design and Synthesis of Phosphite Ligands for Homogeneous Catalysis; 3.1 Introduction; 3.2 Synthesis of phosphites; 3.2.1 Monophosphites; 3.2.2 Diphosphite ligands; 3.2.3 Triphosphites; 3.3 Highlights of catalytic applications of phosphite ligands; 3.3.1 Hydrogenation reactions; 3.3.2 Functionalization of alkenes: hydroformylation and hydrocyanation 3.3.3 Addition of nucleophiles to carbonyl compounds and derivatives3.3.4 Allylic substitution reactions; 3.3.5 Miscellaneous reactions; 3.4 General synthetic procedures; 3.4.1 Symmetrically substituted phosphites; 3.4.2 Nonsymmetrically substituted phosphites; 3.4.3 Phosphites bearing dioxaphospho-cyclic units; References; 4 Phosphoramidite Ligands; 4.1 Introduction; 4.1.1 History; 4.2 Synthesis of phosphoramidites; 4.3 Reactivity of the phosphoramidites; 4.4 Types of phosphoramidite ligands; 4.4.1 Acyclic monodentate phosphoramidites; 4.4.2 Cyclic monodentate phosphoramidites based on diols 4.4.3 Cyclic phosphoramidites based on amino alcohols |
Record Nr. | UNINA-9910810261803321 |
Kamer Paul
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Chichester, West Sussex, United Kingdom, : John Wiley & Sons, Ltd., 2012 | ||
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Lo trovi qui: Univ. Federico II | ||
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Phosphorus, sulfur, and silicon and the related elements [[electronic resource]] |
Pubbl/distr/stampa | [London], : Gordon and Breach |
Disciplina | 546 |
Soggetto topico |
Sulfur compounds
Organosulfur compounds Phosphorus compounds Organophosphorus compounds Silicon compounds Organosilicon compounds |
ISSN | 1563-5325 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Periodico |
Lingua di pubblicazione | eng |
Record Nr. | UNISA-996216298303316 |
[London], : Gordon and Breach | ||
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Lo trovi qui: Univ. di Salerno | ||
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Phosphorus, sulfur, and silicon and the related elements |
Pubbl/distr/stampa | [London], : Gordon and Breach |
Disciplina | 546 |
Soggetto topico |
Sulfur compounds
Organosulfur compounds Phosphorus compounds Organophosphorus compounds Silicon compounds Organosilicon compounds |
ISSN | 1563-5325 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Periodico |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-9910231853803321 |
[London], : Gordon and Breach | ||
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Lo trovi qui: Univ. Federico II | ||
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Reactivity of P-H group of phosphorus based compounds / / Kolio D. Troev |
Autore | Troev Kolio D. |
Pubbl/distr/stampa | London, [England] : , : Academic Press, , 2018 |
Descrizione fisica | 1 online resource (465 pages) |
Disciplina | 546.712 |
Soggetto topico | Phosphorus compounds |
ISBN |
0-12-813835-1
0-12-813834-3 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Front Cover; Reactivity of P-H Group of Phosphorus Based Compounds; Copyright Page; Contents; About the Author; Preface; 1 Acidity and Tautomerization of P-H Group; 1.1 Acidity; 1.2 Tautomerization; 1.2.1 Tautomerization of Phosphine Oxides; 1.2.2 Tautomerization of Hypophosphorous Acid; 1.2.3 Tautomerization of H-Phosphinic Acid; 1.2.4 Tautomerization of H-Phosphonic Acid; References; 2 Reactivity of P-H Group of Phosphines; 2.1 Phosphine; 2.1.1 Methods for Preparation; 2.1.2 Reactivity of P-H Group; 2.1.2.1 Reaction with Metals; 2.1.2.2 Addition Reactions
2.1.2.2.1 Addition to Carbon-Carbon Multiple BondsRadical Addition; Nucleophilic Addition; Catalyzed Hydrophosphination; 2.1.2.2.2 Addition to Carbonyl Group; 2.1.2.3 Nucleophilic Substitution Reactions; 2.2 Primary Phosphines (RPH2); 2.2.1 Methods for Preparation; 2.2.2 Reactivity of P-H Group; 2.2.2.1 Addition Reactions; 2.2.2.1.1 Addition to Carbon-Carbon Multiple Bonds; 2.2.2.1.2 Addition to Carbonyl Group; 2.2.2.2 Cross-Coupling Reactions; 2.2.2.3 Cross-Dehydrogenative Coupling; 2.3 Primary Diphosphines; 2.3.1 Methods for Preparation; 2.3.2 Reactivity of P-H Group; 2.3.2.1 Metalation 2.5.2 Reactivity of P-H Group2.5.2.1 Condensation Reactions; 2.5.2.2 Cross-Coupling Reactions; 2.5.2.2.1 Diphenyldiphosphine PhHP-PHPh; 2.5.2.2.2 Tetraphenyldiphosphane; 2.6 Phosphine-Borane Complexes; 2.6.1 Phosphine-Borane; 2.6.1.1 Methods for Preparation; 2.6.2 Primary Phosphine-Boranes; 2.6.2.1 Methods for Preparation; 2.6.2.2 Reactivity of P-H Group; 2.6.2.2.1 Hydrophosphination; 2.6.2.2.2 Oxidative Addition; 2.6.2.2.3 Cross-Dehydrogenative Coupling; 2.6.2.2.4 Alkylation; 2.6.3 Secondary Phosphine-Boranes; 2.6.3.1 Methods for Preparation; 2.6.3.2 Reactivity of P-H Group 2.6.3.2.1 Alkylation2.6.3.2.2 Hydrophosphination; 2.6.3.2.3 Nucleophilic Substitutions; 2.6.3.2.4 Cross-Coupling Reactions; 2.6.3.2.5 Cross-Dehydrogenative Coupling; Poly(phosphinoborane)s; 2.7 Conclusion; References; 3 Reactivity of P-H Group of Phosphine Oxides; 3.1 Phosphine Oxide; 3.1.1 Methods for Preparation; 3.1.2 Reactivity of P-H Group; 3.2 Primary Phosphine Oxides; 3.2.1 Methods for Preparation; 3.2.2 Reactivity of P-H Group; 3.2.2.1 Dehydration; 3.2.2.2 Addition Reactions; 3.2.2.2.1 Addition to Carbon-Carbon Multiple Bonds; 3.3 Secondary Phosphine Oxides |
Record Nr. | UNINA-9910583094403321 |
Troev Kolio D.
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London, [England] : , : Academic Press, , 2018 | ||
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Lo trovi qui: Univ. Federico II | ||
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Thermal regime of Santa Maria Province, California / / by Colin F. Williams [and three others]. Phosphorus geochemistry, diagenesis, and mass balances of the Miocene Monterey Formation at Shell Beach, California / by Gabriel M. Filippelli and Margaret L. Delaney |
Autore | Williams Colin F. |
Pubbl/distr/stampa | [Reston, Va.] : , : U.S. Department of the Interior, U.S. Geological Survey, , 1994 |
Descrizione fisica | 1 online resource (v, 25, 11 pages) : illustrations |
Collana |
U.S. Geological Survey bulletin
Evolution of sedimentary basins/onshore oil and gas investigations--Santa Maria Province |
Soggetto topico |
Geochemistry - California
Geology, Stratigraphic - Miocene Phosphorus compounds Terrestrial heat flow - California - Santa Maria Basin - Measurement |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Altri titoli varianti | Phosphorus geochemistry, diagenesis, and mass balances of the Miocene Monterey Formation at Shell Beach, California |
Record Nr. | UNINA-9910707692103321 |
Williams Colin F.
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[Reston, Va.] : , : U.S. Department of the Interior, U.S. Geological Survey, , 1994 | ||
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Lo trovi qui: Univ. Federico II | ||
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Untersuchungen zu Synthese, Reaktivität und Bindungsverhältnissen von ausgewählten viergliedrigen Phosphorheterocyclen / / Verena Breuers |
Autore | Breuers Verena |
Pubbl/distr/stampa | Berlin : , : Logos Verlag, , [2015] |
Descrizione fisica | 1 online resource (284 pages) |
Disciplina | 546.712 |
Soggetto topico | Phosphorus compounds |
Soggetto genere / forma | Electronic books. |
ISBN | 3-8325-8794-2 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | ger |
Record Nr. | UNINA-9910467239103321 |
Breuers Verena
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Berlin : , : Logos Verlag, , [2015] | ||
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Lo trovi qui: Univ. Federico II | ||
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